Compound for treating colon cancer and application thereof
A compound and composition technology, applied in the field of medicine, can solve the problems of lower than expected curative effect of colon cancer, toxic and side effects of patients, etc., and achieve the effect of enhancing the anti-tumor effect
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Embodiment 1
[0029] The preparation of embodiment 1 compound of the present invention
[0030] 1. Preparation of liposomes:
[0031] 1) Pre-cool the low-temperature coolant circulation pump to make the cooling temperature below 10°C;
[0032] 2) Take 2.5mgL-α-lysolecithin, 2.5mgL-α-phosphatidylethanolamine, 1mg cholesterol, 2mg cholesterol-peg600, add 4mL absolute ethanol to fully dissolve, transfer to a 25mL round bottom flask;
[0033] (For subsequent preparation of red fluorescent liposomes, 10 μL Atto 532 DOPE dye needs to be added in this step, stock solution concentration: 5 mg / mL)
[0034] 3) Turn on the rotating device, turn on the atmosphere, turn on the switch of the vacuum pump, and seal the joint with glue;
[0035] 4) Set the temperature of the water bath to 40°C, adjust the rotation speed to 150-180r / min, vacuumize and rotate for 1 hour, until the bottom of the flask is covered with a film and almost all the ethanol in the bottle is volatilized;
[0036] 5) Turn off the ro...
Embodiment 2
[0082] Embodiment 2 carries the characterization of black phosphorus quantum dot Adpgk polypeptide liposome
[0083] In order to check whether the prepared Adpgk polypeptide liposomes loaded with black phosphorus quantum dots meet the particle size requirements of drug-loaded nanosystems, their morphology was characterized under a scanning electron microscope, as shown in figure 2 (A represents the topography of the Adpgk polypeptide, B represents the topography of the Adpgk polypeptide liposome loaded with black phosphorus quantum dots, and C and D are the topography of the F127 gel with a concentration of 25%. ).
[0084] After freeze-drying, polypeptide antigens are fragmented and scattered under the scanning electron microscope, and after being encapsulated by liposomes, after freeze-drying, the spherical or ellipsoidal shape similar to liposomes is observed under the scanning electron microscope. And the particle size is shown at about 200nm, which is relatively close to...
Embodiment 3
[0085] Example 3 Cell experiment
[0086] 1. Cell uptake experiment
[0087] 1) Inoculate log phase HeLa or DC2.4 cells of appropriate density into 12-well plates (with cell slides in advance), at 37°C, 5% CO 2 Cultivate overnight in an incubator;
[0088] 2) When the density of adherent cells reaches 70-80% the next day, suck off the old medium;
[0089] 3) Add 750 μL of the culture medium required for the corresponding cells without fetal bovine serum, and then add 250 μL of the corresponding liposome sample to each well, and continue to incubate for 4 hours;
[0090] 4) Aspirate the old culture medium from each well, wash with 1mL 1×PBS buffer solution twice;
[0091] 5) Prepare a film, and observe the uptake effect of the corresponding cells on the liposomes loaded with black phosphorus quantum dots by confocal laser microscopy (CLSM).
[0092] 2. Cytotoxicity test - CCK 8 method
[0093] (1) Detection of cytotoxicity of liposomes loaded with black phosphorus quantum ...
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